To obtain information on the mechanisms responsible of the generation of ragged red fibers (RRF) during aging, we analyzed the mitochondrial genotype of single skeletal muscle fibers of healthy individuals having an age comprised between 45 and 92 years. The sequencing of the D-loop region showed many sequence changes with respect to the Cambridge reference sequence (CRS), in both RRF and normal fibers. These changes were more abundant in RRF and their number increased between 50 and 60, and 61 and 70 years and then remained approximately constant. The analysis of the sequence changes showed that each subject contained one or more changes associated to RRF in positions of D-loop region that either do not change or that change very rare...
<div><p>Aged muscles possess dysfunctional fibers that contain intracellular expansions of somatical...
Several reports described an age-related accumulation of a particular mitochondrial DNA (mtDNA) dele...
The recently discovered aging-dependent large accumulation of point mutations in the human fibroblas...
To have a clearer picture of how mitochondrial damages are associated to aging, a comprehensive stud...
Skeletal muscle–mass loss with age has severe health consequences, yet the molecular basis of the lo...
The aging-dependent large accumulation of specific point mutations, especially the most frequent mut...
AbstractThe A-to-G transition mutation in the tRNALys gene of mitochondrial DNA (mtDNA), characteris...
Mutations in the control region (D-loop) of mitochondrial DNA (mtDNA) have been described in normal ...
Of the ~50 mtDNA point mutations, reported so far, that cause disease in humans, ≥ 35 occur in tRNA...
The age-induced, exponential accumulation of mitochondrial DNA (mtDNA) deletion mutations contribute...
Mitochondrial DNA (mtDNA) mutations are a common cause of human disease and accumulate as part of no...
The small mammalian mitochondrial DNA (mtDNA) is very gene dense and encodes factors critical for ox...
International audienceMitochondrial respiratory chain deteriorates with age, mostly in tissues with ...
Human patients with myoclonic epilepsy with ragged-red fibers (MERRF) suffer from regionalized patho...
International audienceSeveral studies have demonstrated the age-related accumulation of duplications...
<div><p>Aged muscles possess dysfunctional fibers that contain intracellular expansions of somatical...
Several reports described an age-related accumulation of a particular mitochondrial DNA (mtDNA) dele...
The recently discovered aging-dependent large accumulation of point mutations in the human fibroblas...
To have a clearer picture of how mitochondrial damages are associated to aging, a comprehensive stud...
Skeletal muscle–mass loss with age has severe health consequences, yet the molecular basis of the lo...
The aging-dependent large accumulation of specific point mutations, especially the most frequent mut...
AbstractThe A-to-G transition mutation in the tRNALys gene of mitochondrial DNA (mtDNA), characteris...
Mutations in the control region (D-loop) of mitochondrial DNA (mtDNA) have been described in normal ...
Of the ~50 mtDNA point mutations, reported so far, that cause disease in humans, ≥ 35 occur in tRNA...
The age-induced, exponential accumulation of mitochondrial DNA (mtDNA) deletion mutations contribute...
Mitochondrial DNA (mtDNA) mutations are a common cause of human disease and accumulate as part of no...
The small mammalian mitochondrial DNA (mtDNA) is very gene dense and encodes factors critical for ox...
International audienceMitochondrial respiratory chain deteriorates with age, mostly in tissues with ...
Human patients with myoclonic epilepsy with ragged-red fibers (MERRF) suffer from regionalized patho...
International audienceSeveral studies have demonstrated the age-related accumulation of duplications...
<div><p>Aged muscles possess dysfunctional fibers that contain intracellular expansions of somatical...
Several reports described an age-related accumulation of a particular mitochondrial DNA (mtDNA) dele...
The recently discovered aging-dependent large accumulation of point mutations in the human fibroblas...